Organism name | Pterocaulon alopecuroides |
---|---|
Genus | Pterocaulon |
Family | Asteraceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Pterocaulon |
---|---|
Linked NCBI taxonomy ID | 81513 |
Linked level | genus |
Family in NCBI taxonomy | Asteraceae |
---|---|
ID | 4210 |
Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
---|---|
ID | 33090 |
Plant class | asterids |
---|---|
ID | 71274 |
KNApSAcK ID | name | ChEMBL link | CTD link |
# of proteins in
ChEMBL interaction / related OMIM / related KEGG DISEASE |
# of genes in
CTD interaction / related diseases |
KCF-S
cluster |
phytochemical
cluster |
figure |
---|---|---|---|---|---|---|---|---|
C00008636
![]() |
7-O-Prenyltaxifolin
|
No. 276 | No. 14 |
![]() |
||||
C00019845
![]() |
7-(2,3-Dihydroxy-3-methylbutyloxy)-5-hydroxy-5-methoxycoumarin
|
CHEMBL1574904
|
8 / 9 / 7 | No. 579 | No. 25 |
![]() |
||
C00019846
![]() |
7-(2,3-Dihydroxy-3-methylbutyloxy)-5-hydroxy-6-methoxycoumarin
|
No. 579 | No. 25 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P06746 | DNA polymerase beta | Enzyme | C00019845 | 0 / 0 |
P04062 | Glucosylceramidase | Enzyme | C00019845 | 6 / 4 |
P17405 | Sphingomyelin phosphodiesterase | Enzyme | C00019845 | 2 / 2 |
P06280 | Alpha-galactosidase A | Enzyme | C00019845 | 1 / 1 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00019845 | 0 / 0 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00019845 | 0 / 0 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00019845 | 0 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00019845 | 0 / 0 |
OMIM | preferred title | UniProt |
---|---|---|
#301500 | Fabry disease |
P06280
|
#608013 | Gaucher disease, perinatal lethal |
P04062
|
#230800 | Gaucher disease, type i |
P04062
|
#230900 | Gaucher disease, type ii |
P04062
|
#231000 | Gaucher disease, type iii |
P04062
|
#231005 | Gaucher disease, type iiic |
P04062
|
#257200 | Niemann-pick disease, type a |
P17405
|
#607616 | Niemann-pick disease, type b |
P17405
|
#168600 | Parkinson disease, late-onset; pd |
P04062
|
KEGG | name | UniProt |
---|---|---|
H00066 | Lewy body dementia (LBD) |
P04062
(related)
|
H00126 | Gaucher disease |
P04062
(related)
|
H00426 | Defects in the degradation of ganglioside |
P04062
(related)
|
H00810 | Progressive myoclonic epilepsy (PME) |
P04062
(related)
|
H00125 | Fabry disease |
P06280
(related)
|
H00137 | Niemann-Pick disease (NPD) typeA and B |
P17405
(related)
|
H00424 | Defects in the degradation of sphingomyelin |
P17405
(related)
|